SYSTEMATIC REVIEW/META ANALYSIS
|Year : 2017 | Volume
| Issue : 1 | Page : 3-10
|The diagnostic value of polymerase chain reaction for Mycobacterium tuberculosis to distinguish intestinal tuberculosis from crohn's disease: A meta-analysis
Ting Jin1, Baoying Fei2, Yu Zhang3, Xujun He4
1 The First People's Hospital of Xiaoshan District, Hangzhou, Zhejiang, China
2 Department of Gastroenterology, Tongde, Hospital of Zhejiang Province, Zhejiang, China
3 First School of Clinical Medicine Wenzhou Medical University, Wenzhou, Zhejiang, China
4 Department of Gastroenterological Laboratory, Zhejiang Province People's Hospital, Zhejiang, China
Click here for correspondence address and email
|Date of Submission||06-Nov-2015|
|Date of Acceptance||09-Apr-2016|
|Date of Web Publication||27-Jan-2017|
| Abstract|| |
Background/Aim: Intestinal tuberculosis (ITB) and Crohn's disease (CD) are important differential diagnoses that can be difficult to distinguish. Polymerase chain reaction (PCR) for Mycobacterium tuberculosis (MTB) is an efficient and promising tool. This meta-analysis was performed to systematically and objectively assess the potential diagnostic accuracy and clinical value of PCR for MTB in distinguishing ITB from CD. Materials and Methods: We searched PubMed, Embase, Web of Science, Science Direct, and the Cochrane Library for eligible studies, and nine articles with 12 groups of data were identified. The included studies were subjected to quality assessment using the revised Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) tool. Results: The summary estimates were as follows: sensitivity 0.47 (95% CI: 0.42–0.51); specificity 0.95 (95% CI: 0.93–0.97); the positive likelihood ratio (PLR) 10.68 (95% CI: 6.98–16.35); the negative likelihood ratio (NLR) 0.49 (95% CI: 0.33–0.71); and diagnostic odds ratio (DOR) 21.92 (95% CI: 13.17–36.48). The area under the curve (AUC) was 0.9311, with a Q* value of 0.8664. Heterogeneity was found in the NLR. The heterogeneity of the studies was evaluated by meta-regression analysis and subgroup analysis. Conclusions: The current evidence suggests that PCR for MTB is a promising and highly specific diagnostic method to distinguish ITB from CD. However, physicians should also keep in mind that negative results cannot exclude ITB for its low sensitivity. Additional prospective studies are needed to further evaluate the diagnostic accuracy of PCR.
Keywords: Crohn's disease, intestinal tuberculosis, meta-analysis, Mycobacterium tuberculosis, polymerase chain reaction
|How to cite this article:|
Jin T, Fei B, Zhang Y, He X. The diagnostic value of polymerase chain reaction for Mycobacterium tuberculosis to distinguish intestinal tuberculosis from crohn's disease: A meta-analysis. Saudi J Gastroenterol 2017;23:3-10
|How to cite this URL:|
Jin T, Fei B, Zhang Y, He X. The diagnostic value of polymerase chain reaction for Mycobacterium tuberculosis to distinguish intestinal tuberculosis from crohn's disease: A meta-analysis. Saudi J Gastroenterol [serial online] 2017 [cited 2017 Feb 24];23:3-10. Available from: http://www.saudijgastro.com/text.asp?2017/23/1/3/199135
Intestinal tuberculosis (ITB) and Crohn's disease (CD) are both chronic granulomatous inflammatory disorders. Clinical, radiological, endoscopic, and histologic findings are similar between the two disorders, and these disorders have common underlying pathologies., The overall resurgence of TB, which was probably caused by the pandemic of human immunodeficiency virus (HIV) infection and the large wave of population migration, has led to an increase in ITB. As the sixth most common presentation of extrapulmonary TB, ITB is observed in 11% of extrapulmonary TB patients., CD, consisting of chronic relapsing mucosal inflammation that can affect any part of the gastrointestinal tract, results from a dysfunctional innate immune response. The clinical misdiagnosis rate between CD and ITB ranges from 50 to 70%.,,, When ITB is misdiagnosed, unnecessary anti-TB therapy poses a risk of toxicity; in fact, a delayed diagnosis of ITB has been reported to carry a risk of intestinal stenosis, perforation, and septic shock., In addition, severe deterioration or even death may occur if ITB is treated with immunosuppressive therapy. Hence, identifying an accurate and rapid method of distinguishing CD from ITB is necessary and urgent.
Finding evidence of Mycobacterium tuberculosis (MTB) in intestinal tissues is the most credible way of distinguishing CD from ITB. At present, there are various methods that help in confirming the clinical diagnosis of ITB, such as the tuberculin skin test (TST), tuberculin acid-fast bacilli (AFB) staining, MTB culture, and interferon-gamma release assays (IGRAs). Unfortunately, the current routine methods for diagnosing TB are inefficient. For instance, AFB staining is not very sensitive and biopsy culture for MTB is time consuming (requiring 4–8 weeks). In addition, the results of biopsy culture are frequently inaccurate (with accuracy ranging from 25 to 35%). The IGRA is a new method based on MTB-specific antigens identified through genomic research. However, the inability of T-cell-based IGRAs to distinguish between latent and active TB infection  partly limits the assays' utility in disease diagnosis.
Polymerase chain reaction (PCR) is an interesting and promising approach for differentiating ITB from CD, which is also a quick etiological diagnostic method. The procedure of TB-PCR is mainly divided into the following three parts: DNA extraction, DNA amplification, and DNA detection. The target sequence for PCR amplification is IS6110, which is a specific gene segment from M. tuberculosis that has not been detected in other mycobacteria or organisms. Currently, MT-PCR is primarily applied in the clinical samples of fecal and biopsy. Many studies have explored the diagnostic value of PCR, with mixed results. To assess whether PCR can be used as an efficient diagnostic tool, we conducted a meta-analysis of published studies to derive a more precise and comprehensive assessment of the ability of PCR to differentiate ITB from CD.
| Materials and Methods|| |
Data sources and search strategy
We performed a systematic search of PubMed, Embase, Web of Science, Science Direct, and the Cochrane Library for studies published through February 2015. The search terms were as follows: (“tuberculo*” or “TB”) and (“polymerase chain reaction” or “PCR”) and (“Crohn's disease” or “Crohn disease” or “CD”). Additional studies were identified via a manual review of the references to avoid missing potentially relevant studies.
Inclusion and exclusion criteria
The inclusion criteria used in this analysis were as follows: (1) The aim of the study was to explore the value of PCR in distinguishing ITB from CD, (2) the study used recognized criteria to diagnose ITB and CD, (3) the target gene sequence for PCR was IS6110 and the samples were intestinal tissue or feces, (4) the reported primary data were sufficient for separately calculating both the sensitivity and the specificity of PCR in diagnosing ITB or CD samples, and (5) the article was written in English. The exclusion criteria were as follows: (1) Duplicate articles that contained all or a selection of previously published data, (2) reviews, case reports, letters, conference proceedings, and comments, (3) studies without diagnostic criteria information, and (4) articles in a language other than English.
Data extraction and quality assessment
Information on author, year, and country of publication, mean patient age, total number of patients; study type, specimen source, technique, number of true positives, number of false positives, number of false negatives, and number of true negatives was obtained.
The quality of the eight included articles was assessed using the revised Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) tool, which was recommended by the Cochrane Handbook for Systematic Reviews of Diagnostic Test Accuracy. The risk of bias was assessed for each domain, and the applicability of the first three domains was evaluated. Almost none of the articles reported whether the investigators were blinded, so we changed the signal question “Were the index test results interpreted without knowledge of the results of the reference standard?” to “Were the index test results interpreted without the investigators being affected by the results of the reference standard?”
The data extraction and quality assessment were performed independently by two authors (Ting Jin And Yu Zhang). Any discrepancies were discussed with a third author (Baoying Fei) until a consensus was reached.
We used Meta-Disc 1.4 software (XI Cochrane Colloquium, Barcelona, Spain) and Stata 12.0 software (Stata Corporation, College Station, TX, USA) for the data analysis. We calculated Spearman's correlation coefficient, Cochran's Q, and the inconsistency (I2) of the diagnostic odds ratio (DOR) to evaluate the existence of heterogeneity caused by a threshold or non-threshold effect. A P < 0.05 or I2 >50% indicated the existence of heterogeneity. We combined estimates of the sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), and DOR. We also generated a symmetric receiver operator characteristic (SROC) curve to calculate the area under curve (AUC). If no threshold effect was detected but significant heterogeneity existed, regression meta-analysis and subgroup analysis were performed. Publication bias was additionally evaluated using Stata statistical software (version 12.0).
| Results|| |
Selection of studies
We identified 538 studies in our initial search of the databases. We excluded 129 duplicate studies using EndNote software (Thomson Reuters, USA) and 378 irrelevant studies after screening the titles and abstracts; a total of 31 full-text articles remained for full-text screening. Of these publications, six articles contained repeated data and were therefore excluded. Another six articles were excluded because they were case reports, reviews, letters, or conference proceedings, and an additional six articles were excluded because they were unrelated to the purpose of the meta-analysis. Two excluded articles only had an abstract and no full text. Another study was written in the Korean language, and one study did not provide sufficient data to calculate the sensitivity and specificity. Therefore, a total of only nine articles were eligible for further analysis.,,,,,,,, The study selection process is shown in [Figure 1], and the basic characteristics of the selected studies are presented in [Table 1].
|Figure 1: Flowchart of study identification and the inclusion and exclusion criteria|
Click here to view
Evaluation of the study quality
[Figure 2] illustrates the quality assessment of the studies. Five of the nine articles were retrospective studies; therefore, the patient selection criterion was considered unsatisfactory.
|Figure 2: Quality assessment of the nine included studies using the modified QUADAS-2 tool|
Click here to view
Data synthesis and meta-analysis
Spearman's correlation coefficient for PCR was 0.442 (P = 0.151). Cochran's Q and I2 for the DOR were 10.59 (P = 0.4782) and 0.0%, respectively. These values indicate an absence of heterogeneity caused by a threshold or non-threshold effect. Thus, a fixed-effects model was used. The overall diagnostic sensitivity, specificity, PLR, and NLR were 0.47 (95% CI: 0.42–0.51), 0.95 (95% CI: 0.93–0.97), 10.68 (95% CI: 6.98–16.35), and 0.53% (95% CI: 0.48–0.58), respectively [Figure 3]a,[Figure 3]b,[Figure 3]c,[Figure 3]d. The AUC for PCR was 0.9311 [Figure 3]e. Thus, PCR for M. tuberculosis was reasonably accurate in differentiating ITB from CD. Patients with ITB had an approximately 10-fold higher chance of being PCR positive than patients with CD did, and there was no heterogeneity associated with the PLR (heterogeneity Chi-squared = 6.58 (P = 0.8320) and I2 = 0.0%). The heterogeneity Chi-squared for the NLR was 300.87 (P = 0.0000), and the I2 was 96.3%, indicating that there was significant heterogeneity for all of the included studies. We, therefore, used a random-effects model instead of a fixed-effects model. The recalculated pooled NLR was 0.49 (95% CI: 0.33–0.71) [Figure 3]f.
|Figure 3: (a) Pooled sensitivity; (b) Pooled specificity; (c) PLR (fixed-effects model); (d) NLR (fixed-effects model); (e) SROC curve and AUC; (f) NLR (random-effects model)|
Click here to view
Possible sources of heterogeneity
The pooled data showed that there was considerable heterogeneity among the studies. However, Spearman's correlation coefficient indicated that the heterogeneity was not caused by a threshold effect. A meta-regression analysis was used to estimate whether the heterogeneity was caused by differences in the study design and/or the specimen source and/or the assay method of the eligible studies, but the data suggest that these factors were not the source of heterogeneity. The results of the subgroup analysis are shown in [Table 2]. Deeks' funnel plot asymmetry test indicated that there was no publication bias (P = 0.81) [Figure 4].
|Figure 4: Funnel plot for the assessment of potential bias in PCR assays|
Click here to view
| Discussion|| |
ITB and CD are difficult to distinguish, and misdiagnosis of either disorder can have serious repercussions. Thus, an efficient and accurate diagnostic tool that can distinguish between these disorders is a critical need. PCR is a simple and time-saving diagnostic method for detecting ITB. The present study is the first meta-analysis to comprehensively analyze the predictive power of PCR in this context using previously published studies.
In the current study, nine eligible studies, including 369 patients with ITB and 340 patients with CD, were identified. In all of the studies, the patients were diagnosed with their respective diseases using a previously established gold-standard method. We chose to use the QUADAS-2 tool to assess the quality of the studies. Although nearly none of the articles reported whether the investigators were blinded to the study, the cutoff of the PCR machine was pre-specified, and the result of the index test was therefore not judged subjectively. We, therefore, believe that the lack of blinding did not significantly affect the study results.
In our meta-analysis, we calculated Spearman's correlation coefficient and the DOR to estimate whether heterogeneity existed. Our results indicate that there was minimal heterogeneity. Three of the nine articles contained two sets of data due to the use of different PCR assays (conventional or unconventional) and different specimens (fecal samples or biopsy specimens). These studies were analyzed twice, which may have decreased the overall heterogeneity. For this reason, we excluded one dataset from each of the three articles to determine whether the heterogeneity was affected. The recalculated Spearman's correlation coefficient and DOR indicated a lack of heterogeneity caused by a threshold or non-threshold effect. In contrast, the pooled NLR showed significant heterogeneity (P < 0.05).
Next, we further investigated the source of the heterogeneity. Five of the nine articles were retrospective studies, and others were prospective studies, which may affect the heterogeneity. The type of PCR for M. tuberculosis was also different in each study; certain studies used conventional PCR, whereas others used fluorescence quantitative PCR (FQ-PCR), in situ PCR or nested PCR. These varying methods could have increased the heterogeneity. The specimen sources in the articles also differed, including intestinal biopsies, fecal samples, freshly prepared samples, and paraffin-embedded tissue specimens stained with hematoxylin and eosin. These specimen sources may have further added to the heterogeneity. Therefore, we conducted a meta-regression analysis to identify the source of heterogeneity. Unfortunately, our results indicated that the heterogeneity was not caused by the study design, the specimen source, or the assay method. The number of studies analyzed in this meta-analysis was small, which may limit the quality of our analysis. In addition, we speculate that the different test procedures, participant groups, and sample collection times in the studies may have affected the heterogeneity.
PCR for M. tuberculosis was found to be highly specific for ITB but not very sensitive. MTB is not spread evenly or superficially throughout the diseased intestinal tissue, and hence the restricted depth and size of the obtained endoscopic mucosal biopsy specimens and the limited amount of extracted MTB DNA may have been responsible for the low sensitivity. In addition, the use of paraffin-embedded biopsy specimens may have degraded the DNA of the organism, decreasing the yield of the PCR. Furthermore, certain MTB strains do not contain the IS6110 sequence, which may have yielded false negatives. For the false positives, the high prevalence of M. tuberculosis worldwide and incidental infection of CD patients by contaminated water or food consumption may have led to the presence of MTB in CD patients. Moreover, CD patients may co-exist with latent TB infection, which can be activated by immunosuppressive therapy., Another possible problem is contamination of the samples during collection or during handling for the extraction and amplification of MTB DNA.
The pooled sensitivity and specificity do not behave independently when they are pooled from various primary studies to generate separate averages. In the current study, the AUC and DOR were calculated to evaluate the potential diagnostic value of PCR. We found that the AUC for PCR was 0.9311, indicating that PCR for M. tuberculosis is reasonably able to differentiate ITB from CD. The DOR is a single indicator of test accuracy; the pooled DOR in the present meta-analysis was 21.92, further confirming that PCR is useful in distinguishing ITB from CD. Our subgroup analyses indicated that fecal PCR for MTB may have higher diagnostic value, as the DOR of biopsy specimens was 18.15 and that of the fecal samples was 38.24. However, in the literature, there are limited data on the use of fecal samples for detecting MTB DNA to distinguish ITB from CD. Two eligible articles using fecal samples , reported sensitivities of 0.83 and 0.79 and respective specificities of 0.92 and 0.89. In addition, Balamurugan et al. showed that the sensitivity, specificity, PPV, and NPV were 88.8, 100, 100, and 93.7%, respectively. Theoretically, fecal PCR can detect MTB DNA anywhere along the gastrointestinal tract, which makes it less affected by sampling errors. Furthermore, fecal specimens can be obtained non-invasively and conveniently, so patients bear a decreased economic burden and are subjected to less physical discomfort. Thus, fecal PCR is an attractive and promising test that may be used as a complementary approach to identify ITB and CD. Because current research is limited, additional studies evaluating the use of PCR to identify ITB using fecal samples are needed.
Several studies have reported that certain M. tuberculosis strains in India contain either a single copy or no copy of IS6110, especially in the southern part of the country.,, One study  showed that PCR had better sensitivity in detecting both the MPB64 and the IS6110 genes than in detecting the IS6110 gene sequence only. For IS6110-negative strains, more gene segments specific to M. tuberculosis need to be determined for future PCR assays.
We believe that PCR for MTB will be an important tool for the diagnosis of ITB. Future research should focus on the following tasks: (1) Using fresh samples from cases before treatment to improve sensitivity, (2) improving the use of fecal samples for PCR and including additional gene segments, and (3) standardizing the detection method and cutoff values. These tasks will improve the sensitivity and specificity of the test, which will facilitate a more accurate meta-analysis of the diagnostic value of PCR.
This meta-analysis has certain limitations. First, the conference abstracts, letters, studies without sufficient data, and non-English language studies were excluded, which may lead to publication bias; an inflation of accuracy estimates due to the preferential acceptance of papers reporting favorable results. Second, we included studies which used discrepant PCR methods and different samples (feces and tissue), which may affect the accuracy estimates, even though we have discussed this limitation by subgroup analysis. Third, we detected significant heterogeneity across the included studies, but were unable to determine the source by meta-regression. Finally, the number of studies included was limited, and further studies are still needed to evaluate the diagnostic accuracy of PCR.
| Conclusions|| |
Evidence suggests that PCR for M. tuberculosis has potential diagnostic value. In consideration of the low sensitivity, physicians should also consider that negative results cannot exclude ITB and that additional diagnostic tests may be needed. Currently, there is no ideal diagnostic approach for distinguishing ITB from CD. PCR can be viewed as an important complement to conventional tests to help delete confirm the diagnosis, however, additional studies are needed to further evaluate the diagnostic accuracy of PCR.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Kirsch R, Pentecost M, Hall Pde M, Epstein DP, Watermeyer G, Friederich PW. Role of colonoscopic biopsy in distinguishing between Crohn's disease and intestinal tuberculosis. J Clin Pathol 2006;59:840-4.
Arnold C, Moradpour D, Blum HE. Tuberculous colitis mimicking Crohn's disease. Am J Gastroenterol 1998;93:2294-6.
Epstein D, Watermeyer G, Kirsch R. Review article: The diagnosis and management of Crohn's disease in populations with high-risk rates for tuberculosis. Aliment Pharmacol Ther 2007;25:1373-88.
Fei BY, Lv YX, Zheng WH. Fluorescent quantitative PCR of Mycobacterium tuberculosis
for differentiating intestinal tuberculosis from Crohn's disease. Braz J Med Biol Res 2014;47:166-70.
Abgrall S, Del Giudice P, Melica G, Costagliola D; FHDH-ANRS CO4. HIV-associated tuberculosis and immigration in a high-income country: Incidence trends and risk factors in recent years. AIDS 2010;24:763-71.
Donoghue HD, Holton J. Intestinal tuberculosis. Curr Opin Infect Dis 2009;22:490-6.
Kapoor VK. Abdominal tuberculosis. Postgrad Med J 1998;74:459-67.
Friswell M, Campbell B, Rhodes J. The role of bacteria in the pathogenesis of inflammatory bowel disease. Gut Liver 2010;4:295-306.
Almadi MA, Ghosh S, Aljebreen AM. Differentiating intestinal tuberculosis from Crohn's disease: A diagnostic challenge. Am J Gastroenterol 2009;104:1003-12.
Liu TH, Pan GZ, Chen MZ. Crohn's disease. Clinicopathologic manifestations and differential diagnosis from enterocolonic tuberculosis. Chin Med J (Engl) 1981;94:431-40.
Singh V, Kumar P, Kamal J, Prakash V, Vaiphei K, Singh K. Clinicocolonoscopic profile of colonic tuberculosis. Am J Gastroenterol 1996;91:565-8.
Di Placido R, Pietroletti R, Leardi S, Simi M. Primary gastroduodenal tuberculous infection presenting as pyloric outlet obstruction. Am J Gastroenterol 1996;91:807-8.
Morita N, Toki S, Hirohashi T, Minoda T, Ogawa K, Kono S, et al
. Incidence and prevalence of inflammatory bowel disease in Japan: Nationwide epidemiological survey during the year 1991. J Gastroenterol 1995;30(Suppl 8):1-4.
Gan HT, Chen YQ, Ouyang Q, Bu H, Yang XY. Differentiation between intestinal tuberculosis and Crohn's disease in endoscopic biopsy specimens by polymerase chain reaction. Am J Gastroenterol 2002;97:1446-51.
Amarapurkar DN, Patel ND, Rane PS. Diagnosis of Crohn's disease in India where tuberculosis is widely prevalent. World J Gastroenterol 2008;14:741-6.
Leung CC, Yam WC, Ho PL, Yew WW, Chan CK, Law WS, et al
. T-Spot.TB outperforms tuberculin skin test in predicting development of active tuberculosis among household contacts. Respirology 2015;20:496-503.
Pai M, O'Brien R. New diagnostics for latent and active tuberculosis: State of the art and future prospects. Semin Respir Crit Care Med 2008;29:560-8.
Balamurugan R, Venkataraman S, John KR, Ramakrishna BS. PCR amplification of the IS6110 insertion element of Mycobacterium tuberculosis
in fecal samples from patients with intestinal tuberculosis. J Clin Microbiol 2006;44:1884-6.
Whiting PF, Rutjes AW, Westwood ME, Mallett S, Deeks JJ, Reitsma JB, et al
. QUADAS-2: A revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med 2011;155:529-36.
Whiting PF, Weswood ME, Rutjes AW, Reitsma JB, Bossuyt PN, Kleijnen J. Evaluation of QUADAS, a tool for the quality assessment of diagnostic accuracy studies. BMC Med Res Methodol 2006;6:9.
Ramadass B, Chittaranjan S, Subramanian V, Ramakrishna BS. Fecal polymerase chain reaction for Mycobacterium tuberculosis
IS6110 to distinguish Crohn's disease from intestinal tuberculosis. Indian J Gastroenterol 2010;29:152-6.
Jin XJ, Kim JM, Kim HK, Kim L, Choi SJ, Park IS, et al
. Histopathology and TB-PCR kit analysis in differentiating the diagnosis of intestinal tuberculosis and Crohn's disease. World J Gastroenterol 2010;16:2496-503.
Pulimood AB, Peter SJ, Rook GWA, Donoghue HD. In situ
PCR for Mycobacterium tuberculosis
in endoscopic mucosal biopsy specimens of intestinal tuberculosis and Crohn disease. Am J Clin Pathol 2008;129:846-51.
Amarapurkar ND, Patel ND, Amarapurkar AD, Agal A, Baigal R, Gupte P. Tissue polymerase chain reaction in diagnosis of intestinal tuberculosis and Crohn's disease. J Assoc Physicians India 2004;52:863-7.
Gan H, Ouyang Q, Bu H, Li S, Chen D Li G, et al
. Value of polymerase chain reaction assay in diagnosis of intestinal tuberculosis and differentiation from Crohn's disease. Chin Med J (Engl) 1995;108:215-20.
Lei Y, Yi FM, Zhao J, Luckheeram RV, Huang S, Chen M, et al
. Utility of in vitro
interferon-γ release assay in differential diagnosis between intestinal tuberculosis and Crohn's disease. J Dig Dis 2013;14:68-75.
Deeks JJ, Macaskill P, Irwig L. The performance of tests of publication bias and other sample size effects in systematic reviews of diagnostic test accuracy was assessed. J Clin Epidemiol 2005;58:882-93.
Qian L, Van Embden JD, Van Der Zanden AG, Weltevreden EF, Duanmu H, Douglas JT. Retrospective analysis of the Beijing family of Mycobacterium tuberculosis
in preserved lung tissues. J Clin Microbiol 1999;37:471-4.
van Soolingen D, de Haas PE, Hermans PW, Groenen PM, van Embden JD. Comparison of various repetitive DNA elements as genetic markers for strain differentiation and epidemiology of Mycobacterium tuberculosis
. J Clin Microbiol 1993;31:1987-95.
Papa A, Mocci G, Bonizzi M, Felice C, Andrisani G, De Vitis I, et al.
Use of infliximab in particular clinical settings: Management based on current evidence. Am J Gastroenterol 2009;104:1575-86.
Garcia-Vidal C, Rodríguez-Fernández S, Teijón S, Esteve M, Rodríguez-Carballeira M, Lacasa JM, et al
. Risk factors for opportunistic infections in infliximab-treated patients: The importance of screening in prevention. Eur J Clin Microbiol Infect Dis 2009;28:331-7.
Honest H, Khan KS. Reporting of measures of accuracy in systematic reviews of diagnostic literature. BMC Health Serv Res 2002;2:4.
Glas AS, Lijmer JG, Prins MH, Bonsel GJ, Bossuyt PM. The diagnostic odds ratio: A single indicator of test performance. J Clin Epidemiol 2003;56:1129-35.
Das S, Paramasivan CN, Lowrie DB, Prabhakar R, Narayanan PR. IS6110 restriction fragment length polymorphism typing of clinical isolates of Mycobacterium tuberculosis
from patients with pulmonary tuberculosis in Madras, South India. Tuber Lung Dis 1995;76:550-4.
Radhakrishnan I, Manju VK, Kumar AR, Mundayoor S. Implications of low frequency of IS6110 in fingerprinting field isolates of Mycobacterium tuberculosis
from Kerala. J Clin Microbiol 2001;39:1683.
Sahadevan R, Narayanan S, Paramasivan CN, Prabhakar R, Narayanan PR. Restriction fragment length polymorphism typing of clinical isolates of Mycobacterium tuberculosis
from patients with pulmonary tuberculosis in Madras, India, by use of direct repeat probe. J Clin Microbiol 1995;33:3037-9.
Department of Gastroenterology, Tongde Hospital of Zhejiang Province, Hangzhou, Zhejiang
Source of Support: None, Conflict of Interest: None
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2]
| Article Access Statistics|
| Viewed||301 |
| Printed||4 |
| Emailed||0 |
| PDF Downloaded||78 |
| Comments ||[Add] |